It is also interesting to speculate whether reduced dynein heavy chain expression contributes to reduced ciliary beat frequency which is a known effect of cigarette smoking [18], [19].
The application of water conservation measures in upstream reaches contributes to reduced inflows to downstream reaches and structures.
Fgf8 expression in the commissural plate of nestin-Emx2 mice is indistinguishable from wild-type, but Pax6 expression is downregulated in rostral cortical progenitors, suggesting that EMX2 repression of PAX6 specification of rostral identities contributes to reduced rostral areas.
However, to date, the mechanism by which bile aspiration contributes to reduced pulmonary function remains unknown.
However, it is unclear whether LXA4 contributes to reduced cancer risk in humans.
Additionally, medullary hypotonicity significantly contributes to reduced ability of aging kidney to concentrate the urine.
TNF- α cleaves and inactivates SirT1 and thereby contributes to reduced matrix gene expression [ 140].
Inhibition of NF-κB and cadherin-11 by suppression of EPCR also likely contributes to reduced invasion and cartilage degradation by RASFs [ 33, 42].
Thus the chronic intermittent electrical insult inflicted by abnormal ictal and interictal activity in left temporal lobe epilepsy contributes to reduced left anterolateral STC function and significant reorganization of the neural systems supporting language.
Therefore, reduced H3S10 phosphorylation further contributes to reduced Sp-1 recruitment.
Loss of synapsin I appears to preferentially affect inhibitory neurons and, like Gabra5, produces a phenotype of increased excitability in knockout mice., Thus, reduced Syn1 gene expression likely contributes to reduced inhibitory drive in the hippocampus.
